Documenting the Corneal Phenotype Associated with the MIR184 c.57C>T Mutation

Liknande verk

• A Single-Base Substitution in the Seed Region of miR-184 Causes EDICT Syndrome
  av: Iliff, Benjamin W., et al.
  Publicerad: (2012)
• Independent origin of c.57C>T mutation in MIR184 associated with inherited corneal and lens abnormalities
  av: Bykhovskaya, Yelena, et al.
  Publicerad: (2014)
• The genetics of Fuchs′ corneal dystrophy
  av: Iliff, Benjamin W, et al.
  Publicerad: (2012)
• C.57 C>T mutation in MIR 184 is responsible for congenital cataracts and corneal abnormalities in a five-generation family from Galicia, Spain
  av: Bykhovskaya, Yelena, et al.
  Publicerad: (2015)
• Mutations in AGBL1 Cause Dominant Late-Onset Fuchs Corneal Dystrophy and Alter Protein-Protein Interaction with TCF4
  av: Riazuddin, S. Amer, et al.
  Publicerad: (2013)